FDA 510(k) Application Details - K211640

Device Classification Name	Hearing Aid, Bone Conduction   More FDA Info for this Device
510(K) Number	K211640
Device Name	Hearing Aid, Bone Conduction
Applicant	Oticon Medical AB Datavagen 37B Askim SE-436 32 SE Other 510(k) Applications for this Company
Contact	Anja Ravn Other 510(k) Applications for this Contact
Regulation Number	874.3300   More FDA Info for this Regulation Number
Classification Product Code	LXB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/27/2021
Decision Date	08/10/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	EN - Ear, Nose, & Throat
Review Advisory Committee	EN - Ear, Nose, & Throat
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review